Rigid dinuclear ruthenium-arene complexes showing strong DNA interactions

被引:26
作者
Wu, Qi [1 ]
Liu, Liu-Yi [2 ]
Li, Shunli [1 ]
Wang, Fang-Xin [2 ]
Li, Ji [1 ]
Qian, Yong [1 ]
Su, Zhi [1 ]
Mao, Zong-Wan [2 ]
Sadler, Peter J. [3 ]
Liu, Hong-Ke [1 ]
机构
[1] Nanjing Normal Univ, Jiangsu Collaborat Innovat Ctr Biomed Funct Mat, Sch Chem & Mat Sci, Nanjing 210046, Jiangsu, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem, MOE Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Guangdong, Peoples R China
[3] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
ANTICANCER ACTIVITY; ANION-EXCHANGE; CELL-CYCLE; BINDING; CYTOTOXICITY; APOPTOSIS; RECOGNITION; DIVERSITY; AFFINITY; RH(III);
D O I
10.1016/j.jinorgbio.2018.08.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Six novel dinuclear Ru(II)-arene complexes [Ru-2(eta(6)-p-cymene)(2)(1,3-bib)(2)Cl-2] x(2)center dot Solvent (X = Cl-, I- (2), NO3- (3), BF4- (4), PF5- (5), CF3SO3- (6); 1,3-bib = 1,3-di(1H-imidazol-1-yl) benzene) were synthesized and fully characterized by FT-IR, H-1 NMR, ESI-MS, Elemental Analysis (EA) and Powder X-ray Diffraction (PXRD). Single crystal X-ray diffractions studies showed that 3 and 4 have rigid bowl-like structures, where one counter-anion (NO3- for 3 and BF4- for 4) was trapped inside the cavity to balance the charge, respectively. Even complexes 1-6 showed only moderate or little anti-proliferative activity toward cancer cells, strong interactions with DNA molecules through intercalation, however, were confirmed by UV-Vis, CD and fluorescence spectroscopy. Apoptosis and cell cycle arrest studies for complex 2 with cancer A549 cells indicated concentration-dependent late apoptosis and the G1/G0 phase arrest. Interactions with the tripeptide glutathione (gamma-L-Glu-L-Cys-Gly, GSH) might explain the relatively low antiproliferative potency of these complexes. This class of rigid dinuclear cations hold potential as DNA-targeting anticancer agents if their uptake and delivery could be under controlled.
引用
收藏
页码:30 / 39
页数:10
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